Haplotype-Specific DNA Methylation
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GWAS Disease/Phenotype
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ATXN2
hits 4
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1
rs3184504
chr12:111884607-111884608
genes 7
GWAS disease/phenotype 10
rs3184504
LD Block:
chr12:111358233-112615538
Genes:
ATXN2
BRAP
C12orf51
LOC100101246
NAA25
PTPN11
SH2B3
GWAS Disease/Phenotype:
Autoimmune hepatitis type-1
Beta-2 microglubulin plasma levels
Diastolic blood pressure
Eosinophil counts
Hypothyroidism
Platelet counts
Red blood cell traits
Systolic blood pressure
Type 1 diabetes
Type 1 diabetes autoantibodies
2
rs10774625
chr12:111910218-111910219
genes 3
GWAS disease/phenotype 1
rs10774625
LD Block:
chr12:111358233-112615538
Genes:
ATXN2
PTPN11
SH2B3
GWAS Disease/Phenotype:
Retinal vascular caliber
3
rs653178
chr12:112007755-112007756
genes 3
GWAS disease/phenotype 7
rs653178
LD Block:
chr12:111358233-112615538
Genes:
ATXN2
PTPN11
SH2B3
GWAS Disease/Phenotype:
Blood pressure
Celiac disease
Celiac disease and Rheumatoid arthritis
Chronic kidney disease
Diastolic blood pressure
Serum thyroid peroxidase antibody positivity
Urate levels
4
rs11065987
chr12:112072423-112072424
genes 5
GWAS disease/phenotype 7
rs11065987
LD Block:
chr12:111358233-112615538
Genes:
ATXN2
BRAP
PTPN11
SH2B3
TRAFD1
GWAS Disease/Phenotype:
Cholesterol, total
Coronary artery disease or ischemic stroke
Coronary artery disease or large artery stroke
Hematocrit
Hemoglobin
LDL cholesterol
Tetralogy of Fallot
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